Results 71 to 80 of about 16,068 (216)

Atrial Cardiopathy and Sympatho-Vagal Imbalance in Cryptogenic Stroke: Pathogenic Mechanisms and Effects on Electrocardiographic Markers

Frontiers in Neurology, 2018
Recently, atrial cardiopathy has emerged as possible pathogenic mechanism in cryptogenic stroke and many electrocardiographic (ECG) markers have been proposed in order to detect an altered atrial substrate at an early stage. The autonomic nervous system (
Maurizio Acampa, Pietro E. Lazzerini, Giuseppe Martini   +2 more
doaj   +1 more source

Safety and Efficacy of MA01‐100: A Prospective Multicenter Trial of China's First Domestic Implantable Cardiac Monitor

Pacing and Clinical Electrophysiology, EarlyView.
ABSTRACT Background Unexplained syncope and palpitations are common chief complaints in the outpatient department of cardiology. Their sporadic and unpredictable poses significant diagnostic challenges. Implantable cardiac monitors (ICMs) can monitor arrhythmia events efficiently, and can overcome the shortcomings of traditional electrocardiogram (ECG)
Lei Xu, Zhuocong Xu, Shengmei Qin, Lei Zhang, Jin Bai, Wei Wang, Ruogu Li, Jingfeng Wang, Huanyi Zhang, Hui Li, Wei Xu, Yang Liu, Shaocong Wang, Lichuan Ping, Xueying Chen, Yangang Su, Junbo Ge   +16 more
wiley   +1 more source

Effects of cerebral small vessel disease on the outcomes in cryptogenic stroke with active cancer

Scientific Reports, 2021
Cerebral small vessel diseases (cSVDs) affect the prognosis of various types of ischemic stroke. Therefore, we evaluated the association between cSVD and the prognosis of cryptogenic stroke patients with active cancer. We enrolled patients diagnosed with
Ki-Woong Nam, Hyung-Min Kwon, Yong-Seok Lee, Jeong-Min Kim, Sang-Bae Ko   +4 more
doaj   +1 more source

Hereditary Thrombotic Thrombocytopenic Purpura Associated With Recurrent Strokes and Prominent Nervous System Involvement in a Young Chinese Female

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Hereditary thrombotic thrombocytopenic purpura (TTP) is a rare autosomal recessive inherited disease caused by an ADAMTS1 gene mutation, resulting in absence or severe deficiency of plasma ADAMTS13 activity. The common causes include infection, inflammation, or pregnancy.
Wanying Liu, Jiaying Wu, Xi Ming, Qi Zhang, Delian Zhou, Rubing Zheng, Mi Zhou, Zhen Shang, Liting Chen, Xiaojian Zhu, Yi Xiao   +10 more
wiley   +1 more source

Impairment of left atrial function and cryptogenic stroke: Potential insights in the pathophysiology of stroke in the young

International Journal of Cardiology: Heart & Vasculature, 2020
Background: Stroke is one of the leading causes of morbidity and mortality with a significant percentage classified as cryptogenic. Left atrial (LA) remodelling, a substrate for atrial fibrillation (AF) and stroke development, may play a role in ...
Aditya Bhat, Shaun Khanna, Henry H. Chen, Lina Lee, Gary C.H. Gan, Kazuaki Negishi, C. Raina MacIntyre, Maria Carmo P. Nunes, Timothy C. Tan   +8 more
doaj   +1 more source

Burden of Liver Disease Among Individuals With Turner Syndrome and Klinefelter Syndrome: A Comprehensive Perspective

Chronic Diseases and Translational Medicine, Volume 12, Issue 1, Page 39-48, March 2026.
ABSTRACT The liver is increasingly recognized as a major regulator of systemic cardio‐renal‐metabolic health. Evidence is mounting that sex‐chromosome dosage per se itself, independent of gonadal sex hormones, modulates hepatic physiology and liver disease risk.
Mohamad Jamalinia, Amedeo Lonardo, Ralf Weiskirchen   +2 more
wiley   +1 more source

Debatable issues in automated ECG reporting [PDF]

, 2017
Although automated ECG analysis has been available for many years, there are some aspects which require to be re-assessed with respect to their value while newer techniques which are worthy of review are beginning to find their way into routine use.
Abächerli, Roger, Albert, David E., Drew, Barbara, Hodges, Morrison, Kligfield, Paul, Macfarlane, Peter W., Mason, Jay W., Sommargren, Claire E., van Dam, Peter   +8 more
core   +1 more source

A Meta‐Analysis to Unveil the Diagnostic Gaps in Anderson–Fabry Disease in Women

Journal of Inherited Metabolic Disease, Volume 49, Issue 2, March 2026.
ABSTRACT Anderson–Fabry disease (AFD) is an X‐linked lysosomal storage disorder caused by mutations in the GLA gene, leading to deficient α‐galactosidase A activity. Although historically considered a male disease, it is now recognized that heterozygous women can present with a wide range of symptoms. However, diagnosis in women remains challenging, as
L. Lenzini, G. Pintus, G. Gugelmo, A. P. Burlina, G. P. Fadini, A. B. Burlina, N. Vitturi   +6 more
wiley   +1 more source

Different expression patterns of inflammation-related genes and serum microRNAs in young-onset ischemic stroke

Scientific Reports
Brain ischemia results in the activation of a cascade of inflammatory responses, contributing to the pathogenesis of stroke. This study aimed to assess the patterns of possible changes in the expression of specific inflammation-associated protein ...
Riina Vibo, Karl Jõgi, Anu Remm, Ana Rebane, Janika Kõrv   +4 more
doaj   +1 more source

Does Atrial Septal Anatomy Still Matter in the Etiological Evaluation of Ischemic Stroke Beyond the Age of 60?

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Patent foramen ovale (PFO) is causally associated with stroke in some patients younger than 60 years, especially when it is large or associated with an atrial septal aneurysm (ASA).
Antoine Dusonchet, Olivier Varenne, Tania Puscas, Malika Saadi, Albert Hagege, David Calvet, Jean‐Louis Mas, Guillaume Turc   +7 more
doaj   +1 more source